Metal telluride nanosheets by scalable solid lithiation and exfoliation.

Transition metal tellurides (TMTs) have been ideal materials for exploring exotic properties in condensed-matter physics, chemistry and materials science1-3. Although TMT nanosheets have been produced by top-down exfoliation, their scale is below the gram level and requires a long processing time, restricting their effective application from laboratory to market4-8. We report the fast and scalable synthesis of a wide variety of MTe2 (M = Nb, Mo, W, Ta, Ti) nanosheets by the solid lithiation of bulk MTe2 within 10 min and their subsequent hydrolysis within seconds. Using NbTe2 as a representative, we produced more than a hundred grams (108 g) of NbTe2 nanosheets with 3.2 nm mean thickness, 6.2 µm mean lateral size and a high yield (>80%). Several interesting quantum phenomena, such as quantum oscillations and giant magnetoresistance, were observed that are generally restricted to highly crystalline MTe2 nanosheets. The TMT nanosheets also perform well as electrocatalysts for lithium-oxygen batteries and electrodes for microsupercapacitors (MSCs). Moreover, this synthesis method is efficient for preparing alloyed telluride, selenide and sulfide nanosheets. Our work opens new opportunities for the universal and scalable synthesis of TMT nanosheets for exploring new quantum phenomena, potential applications and commercialization.

Functions of potassium channels blocked by low micromolar 4-aminopyridine in the crayfish nervous system.

4-aminopyridine (4-AP) is a potassium channel blocker that has been used to treat patients with multiple sclerosis and Lambert-Eaton disease. The concentration of this drug in the blood of patients was estimated to be in low or submicromolar range. Animal studies have shown that 4-AP at such low concentration selectively blocks a subset of channels in Kv1 or Kv3 families. The crayfish opener neuromuscular junction and ventral superficial flexor (VSF) preparations were used to examine functions of K+ channels blocked by low concentrations of 4-AP. At opener motor axons, intracellular recordings show that 4-AP could increase action potential (AP) amplitude, duration, and after-depolarization (ADP) at 10 µM. As 4-AP concentration was increased, in twofold steps, AP amplitude did not increase further up to 5 mM. AP duration and ADP increased significantly mainly in two concentration ranges, 10-50 µM and 1-5 mM. The effects of 50 µM 4-AP on the VSF were less consistent than that observed at the opener motor axons. 4-AP did not change AP amplitude of motor axons recorded with an extracellular electrode and change in AP repolarizing potential was observed in ∼25% of the axons. EPSP recorded simultaneously with AP showed an increase in amplitude with 4-AP treatment only in 30% of the axon-EPSP pairs. 4-AP also increased firing frequencies of ∼50% of axons. In four animals, 4-AP "awakened" the firing of APs from an axon that was silent before the drug. The mixture of positive and negative 4-AP effects summarized above was observed in the same VSF preparations in all cases (n = 8). We propose that there is a significant diversity in the density 4-AP-sensitive potassium channels among motor axons of the VSF. Functional significance in the differences of 4-AP sensitivity of the two motor systems is discussed.

Stable Ti3C2Tx MXene-Boron Nitride Membranes with Low Internal Resistance for Enhanced Salinity Gradient Energy Harvesting.

Extracting salinity gradient energy through a nanomembrane is an efficient way to obtain clean and renewable energy. However, the membranes with undesirable properties, such as low stability, high internal resistance, and low selectivity, would limit the output performance. Herein, we report two-dimensional (2D) laminar nanochannels in the hybrid Ti3C2Tx MXene/boron nitride (MXBN) membrane with excellent stability and reduced internal resistance for enhanced salinity gradient energy harvesting. The internal resistance of the MXBN membrane is significantly reduced after adding BN in a pristine MXene membrane, due to the small size and high surface charge density of BN nanosheets. The output power density of the MXBN membrane with 44 wt % BN nanosheets reaches 2.3 W/m2, almost twice that of a pristine MXene membrane. Besides, the output power density can be further increased to 6.2 W/m2 at 336 K and stabilizes for 10 h at 321 K, revealing excellent structure stability of the membrane in long-term aqueous conditions. This work presents a feasible method for improving the channel properties, which provides 2D layered composite membranes in ion transport, energy extraction, and other nanofluidic applications.

2D Nb4 N5 Nanosheets Synthesized by a Template Method.

Niobium nitrides possess superconductivity and stable chemical stability, which render them desirable candidates for energy storage. Therefore, they deserve exploration for potential energy storage applications. Here we report on the synthesis of 2D Nb4 N5 nanosheets by ammonization of NbS2 nanosheets as templates at 700 °C. The obtained 2D Nb4 N5 nanosheets retain their hexagon shape and display a porous structure with a pore size of 3.716 nm. These 2D Nb4 N5 nanosheets exhibit capacitor behavior as electrode materials for energy storage. This study opens a new avenue in synthesizing 2D materials based on 2D templates.

Controlled Design of a Robust Hierarchically Porous and Hollow Carbon Fiber Textile for High-Performance Freestanding Electrodes.

For most carbon-based materials, hierarchical porous structure including well-defined macropores, mesopores, and micropores is commonly seen in 3D aerogels, monoliths, or some carbothermic natural biomass. However, because of the filiform character and long draw ratio, it is difficult to achieve such pore network as well as attain excellent mechanical performance in a 1D single carbon fiber system. To address this issue, an innovative hierarchical porous and hollow carbon textile (HPHCT) is developed via the "dynamic template (KOH, SiO2, and Al2O3) calcination" strategy. Unlike conventional one-step activated carbonized fiber simply with meso or micropores, the fabricated textile generates honeycomb-like macropores uniformly spreading on fiber surface. More importantly, the ultra-lightweight yet flexible HPHCT is mechanically robust, superior to ordinary carbonized one. In addition, it delivers high capacitance of maximum 220 F g-1 as well as keeping long term stability with 100% retention after 10 000 cycles as freestanding electrodes in supercapacitor. Meanwhile, the all-solid integrated symmetric HPHCT supercapacitors demonstrates its high potential in powering electronics for wearable energy storage application.

Ultrafast, Stable Ionic and Molecular Sieving through Functionalized Boron Nitride Membranes.

Porous membranes play an important role in the separation technologies such as gas purification, solute nanofiltration, and desalination. An ideal membrane should be thin to maximize permeation speed, have optimum pore sizes to maximize selectivity, and be stable in various harsh conditions. Here, we show that the nanometer-thick membrane prepared by means of filtration of functionalized boron nitride (FBN) water suspensions can block solutes with hydrated radii larger than 4.3 Å in water. The FBN membranes with abundant nanochannels reduce the path length of ions. As molecular sieves, the FBN membrane can permeate small ions at an ultrahigh rate-a 25-fold enhancement compared with that of its theoretical diffusion rate and much higher than the graphene oxide membrane. Importantly, the FBN membrane exhibits excellent permeability even when it is immersed in acidic, alkaline, and basic salts solutions because of its intrinsic chemical stability. The molecular dynamics simulations further confirmed that the nanocapillaries formed within the FBN membrane in the hydrated state were responsible for high permeation performance. The simple vacuum filtration fabricated FBN membrane with angstrom-sized channels and ultrafast permeation of ions promises great potential applications in the areas of barrier separation and water purification.